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Pyridine → 3-(3,5-Dimethylpyrazol-1-yl)-5-nitro-1,2-benzisothiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 3,5-Dimethylpyrazole | HCID 6210 | — |
| 反応物 | 1,2-Benzisothiazole, 3-chloro-5-nitro- | HCID 198098 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 3-(3,5-Dimethylpyrazol-1-yl)-5-nitro-1,2-benzisothiazole | HCID 20634266 | 43.8% |
反応手順
A mixture of 3-chloro-5-nitrobenzisothiazole (5.3 g, mmol), 3,5-dimethylpyrazole (2.40 g, 25.0 mmol) and pyridine is stirred overnight at reflux, cooled to room temperature and diluted with ethyl acetate. The resultant mixture is filtered and the filtrate is washed with three portions of 10% hydrochloric acid and one portion of water. The organic layer is dried over anhydrous magnesium sulfate and concentrated in vacuo to afford the title compound (2.85 g, 43.8%) which is identified by NMR spectral analysis.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06706663B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-2faec26a94d54e92a133e6d5e439322b |
| 出典メモ | uspto-grants-2004_03 |